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Study Start Up Associate II

  1. Bangalore, Chennai, Bengaluru
JR125518
  1. Study Start Up
  2. ICON Full Service & Corporate Support
  3. Hybrid: Office/Remote
  1. Bangalore, Chennai, Bengaluru
JR125518
  1. Study Start Up
  2. ICON Full Service & Corporate Support
  3. Hybrid: Office/Remote

About the role

This vacancy has now expired. Please see similar roles below...

Study Start-Up Associate-II

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of inNvative treatments and therapies.

Roles & Responsibilities:

You will be a key member of the Study Start-Up team. You will:

  • Interact successfully with both internal and external customers

  • Exhibit good decision making skills, utilizing all available resources to achieve positive outcomes

  • Communicate with investigative sites and internal team members to predict timelines for site activation and ensure all activation requirements are met

  • Work on local IRB submissions

  • Review and customization if ICFs

  • Collect and review essential regulatory documents needed for site activation

  • Identify and escalate issues before they become critical

  • Adjust quickly to the changes of a dynamic organization

  • Update systems in a timely and accurate way

  • Be highly organized in an environment with shifting priorities

  • Analyse data and metrics relating to the site activation pathway

  • Learn and utilize various reporting tool

Your profile

  • Minimum of 4 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.

  • Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.

  • Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.

  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.

#LI-AB2

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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